The following data is part of a premarket notification filed by Dentsply Intl. with the FDA for Ultracrown(tm) Pd Dental Alloy.
Device ID | K913232 |
510k Number | K913232 |
Device Name: | ULTRACROWN(TM) PD DENTAL ALLOY |
Classification | Alloy, Other Noble Metal |
Applicant | DENTSPLY INTL. 570 WEST COLLEGE AVE. P.O. BOX 872 York, PA 17405 |
Contact | Jeffery Lehn |
Correspondent | Jeffery Lehn DENTSPLY INTL. 570 WEST COLLEGE AVE. P.O. BOX 872 York, PA 17405 |
Product Code | EJS |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-07-22 |
Decision Date | 1991-09-06 |